HCID 19356974, compound → HCID 18663062, compound

HRID 1956227Notes

Reaction equation

HRID 1956227 reaction equation
C1(O[C:8](=[O:21])[NH:9][C:10]2[C:11]([O:19][CH3:20])=[N:12][C:13]([CH3:18])=[C:14]([CH2:16][CH3:17])[CH:15]=2)C=CC=CC=1.[C:22]1([N:36]2[CH2:41][CH2:40][NH:39][CH2:38][CH2:37]2)[C:35]2[C:26](=[CH:27][C:28]3[C:33]([CH:34]=2)=[CH:32][CH:31]=[CH:30][CH:29]=3)[CH:25]=[CH:24][CH:23]=1>>[CH2:16]([C:14]1[CH:15]=[C:10]([NH:9][C:8]([N:39]2[CH2:38][CH2:37][N:36]([C:22]3[C:35]4[C:26](=[CH:27][C:28]5[C:33]([CH:34]=4)=[CH:32][CH:31]=[CH:30][CH:29]=5)[CH:25]=[CH:24][CH:23]=3)[CH2:41][CH2:40]2)=[O:21])[C:11]([O:19][CH3:20])=[N:12][C:13]=1[CH3:18])[CH3:17]

Participants

3

Reactant 2

HCID 19356974HCID 19356974, compoundHCID 19357010Phenyl N-(5-ethyl-2-methoxy-6-methylpyridin-3-yl)carbamate

Product 1

HCID 18663062HCID 18663062, compoundYield 57%

Procedure

Phenyl-N-(5-ethyl-2-methoxy-6-methylpyridin-3-yl)carbamate and 1-(1-anthryl)piperazine were reacted by the same way with the example 1 to obtain the titled compound.

Sources & evidence

ORD record
ord-cc0de08c939048a880e0b8d535ec5eb0
Source dataset
uspto-grants-1998_07
Patent number
US05780472

Reaction notes

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